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CYCLOBUTYL 4-METHOXYPHENYL KETONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100121-80-0

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100121-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100121-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,2 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100121-80:
(8*1)+(7*0)+(6*0)+(5*1)+(4*2)+(3*1)+(2*8)+(1*0)=40
40 % 10 = 0
So 100121-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O2/c1-14-11-7-5-10(6-8-11)12(13)9-3-2-4-9/h5-9H,2-4H2,1H3

100121-80-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclobutyl-(4-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names Cyclobutyl-(4-methoxy-phenyl)-methanone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100121-80-0 SDS

100121-80-0Relevant academic research and scientific papers

Electrochemical [4+2] Annulation-Rearrangement-Aromatization of Styrenes: Synthesis of Naphthalene Derivatives

Ma, Yueyue,Lv, Jufeng,Liu, Chengyu,Yao, Xiantong,Yan, Guoming,Yu, Wei,Ye, Jinxing

, p. 6756 - 6760 (2019/04/17)

We report the first electrochemical strategy to synthesize functionalized naphthalene derivatives through [4+2] annulation—rearrangement–aromatization from styrenes under mild conditions. The electrolysis does not require metals, oxidants and high valence substrates, indicating the atom and step-economy ideals. The dehydrodimer produced through [4+2] cycloaddition of 4-methoxy α-methyl styrene is isolated and proved to be the key intermediate for the following oxydehydrogenation to form carbon cation, which undergoes rearrangement–aromatization to afford the final products. This reaction represents a powerful access to construct multi-substituted naphthalene blocks in a single step.

Fragrance and flavour compositions

-

, (2008/06/13)

The invention relates to phenyl-cycloalkanes of formula (I) wherein the groups R1 to R6 are defined in the specification.

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